Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL278363 | 0.97 | — | — | |
| Hydrochloric Acid SCHEMBL11036693 | 0.76 | — | — | |
| SCHEMBL10392179 | 0.74 | HTT (0.31) | — | |
| Hydrochloric Acid SCHEMBL28283206 | 0.73 | ALDH1A1 (0.32) | — | |
| SCHEMBL11033003 | 0.72 | — | — | |
| SCHEMBL12442210 | 0.72 | — | — | |
| SCHEMBL2054270 | 0.72 | — | — | |
| SCHEMBL4252188 | 0.71 | — | — | |
| Hydrochloric Acid SCHEMBL11110998 | 0.70 | — | — | |
| SCHEMBL24243329 | 0.70 | CA1 (0.33) | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 18 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-7476762-B2 | Methods for preparing sulfonamide compounds | WYETH (US) | 2009-01-13 | — | — | US | claimed |
| US-20070249723-A1 | Methods for preparing sulfonamide compounds | WYETH (US) | 2007-10-25 | — | — | US | claimed |
| EP-0581613-A1 | Process for preparing N,O-dialkylhydroxycarbamic acid esters | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1994-02-02 | — | — | EP | claimed |
| JP-6135918-A | — | — | None | — | — | JP | disclosed |
| JP-6128206-A | — | — | None | — | — | JP | disclosed |
| US-20090082591-A1 | METHODS FOR PREPARING SULFONAMIDE COMPOUNDS | WYETH (US) | 2009-03-26 | — | — | US | disclosed |
| US-7476762-B2 | Methods for preparing sulfonamide compounds | WYETH (US) | 2009-01-13 | — | — | US | disclosed |
| US-20070249723-A1 | Methods for preparing sulfonamide compounds | WYETH (US) | 2007-10-25 | — | — | US | disclosed |
| US-5510511-A | REACTING HYDROXYLAMINE AND DIHYDROCARBYL CARBONATE WITH COOLING IN PRESENCE OF BASIC COMPOUND, ALKYLATING TO FORM N,O-DIALKYLHYDROXYCARBAMIC ACID ESTER | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1996-04-23 | — | — | US | disclosed |
| US-5510511-A | REACTING HYDROXYLAMINE AND DIHYDROCARBYL CARBONATE WITH COOLING IN PRESENCE OF BASIC COMPOUND, ALKYLATING TO FORM N,O-DIALKYLHYDROXYCARBAMIC ACID ESTER | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1996-04-23 | — | — | US | disclosed |
| EP-0692469-A1 | Process for recovering N,O-dialkylhydroxycarbamic acid ester | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1996-01-17 | — | — | EP | disclosed |
| US-5387602-A | Antiinflammatory agents | ORTHO PHARMACEUTICAL CORPORATION (US) | 1995-02-07 | — | — | US | disclosed |
| JP-H06135918-A | METHOD FOR SEPARATING N,O-DIALKYLHYDROXYLAMINE HYDROCHLORIDE | MITSUI PETROCHEM IND LTD | 1994-05-17 | — | — | JP | disclosed |
| JP-H06128206-A | METHOD FOR PURIFYING N,O-DIALKYLHYDROXYLAMINE HYDROCHLORIDE | MITSUI PETROCHEM IND LTD | 1994-05-10 | — | — | JP | disclosed |
| US-5298521-A | Anti-inflammatory agent | ORTHO PHARMACEUTICAL CORPORATION (US) | 1994-03-29 | — | — | US | disclosed |
| EP-0581613-A1 | Process for preparing N,O-dialkylhydroxycarbamic acid esters | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1994-02-02 | — | — | EP | disclosed |
| EP-0581613-A1 | Process for preparing N,O-dialkylhydroxycarbamic acid esters | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1994-02-02 | — | — | EP | disclosed |
| US-4914124-A | ADMINISTERING NEMATOCIDES | BAYER AKTIENGESELLSCHAFT (DE) | 1990-04-03 | — | — | US | disclosed |